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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
eye disease +     
Abnormalities, Drug-Induced +   
Abnormalities, Severe Teratoid +   
Absence of Nasal Bones 
Absence of Vagina 
Accessory Pancreas 
agenesis of corpus callosum, cardiac, ocular, and genital syndrome  
Agenesis of Gallbladder  
AICAR Transformylase Inosine Monophosphate Cyclohydrolase Deficiency  
Aicardi syndrome 
Amastia +   
amblyopia +   
ancylostomiasis +  
Arrhinia 
Asthenopia  
Atlanto-Axial Fusion 
baylisascariasis 
blindness +   
Bresheck/Bresek Syndrome 
Cardiovascular Abnormalities +   
Caudal Duplication Anomaly  
Cerebellar, Ocular, Craniofacial, and Genital Syndrome  
chromosomal disease +   
Cogan syndrome +   
Complete Absence of Bile and Pancreatic Ducts 
Congenital Aural Atresia  
congenital diaphragmatic hernia +   
Congenital Microtia +   
Congenital Stridor 
conjunctival disease +   
corneal disease +   
Crane-Heise Syndrome 
cysticercosis +  
Deal Barratt Dillon Syndrome 
Digestive System Abnormalities +   
dipetalonemiasis 
Encephalocraniocutaneous Lipomatosis  
Eye Abnormalities +   
Congenital absence of or defects in structures of the eye; may also be hereditary.
eye accommodation disease +  
eye adnexa disease +   
eye degenerative disease +   
Eye Hemorrhage +   
Eye Infections +   
Eye Injuries +   
Eye Manifestations +   
Eye Neoplasms +   
eyelid disease +   
Familial Cryptotia 
Familial Laryngeal Web 
fundus dystrophy +   
glaucoma +   
globe disease +   
gonorrhea +  
Hereditary Eye Diseases +   
Hereditary Sensorimotor Neuropathy with Upper Motor Neuron, Visual Pathway and Autonomic Disturbance 
Hernandez Fragoso Syndrome 
Hydrocephalus, Skeletal Anomalies, and Mental Disturbance 
lacrimal apparatus disease +   
Laryngeal Cleft 
lens disease +   
leprosy +   
loiasis 
Lymphatic Abnormalities +   
Marfan syndrome +   
Mayer-Rokitansky-Kuster-Hauser syndrome +   
microphthalmia +   
Mollica Pavone Antener Syndrome 
Mondini Dysplasia  
MORM Syndrome  
Multiple Abnormalities +   
Musculoskeletal Abnormalities +   
Nervous System Malformations +   
NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND VARIABLE INTELLECTUAL AND BEHAVIORAL ABNORMALITIES  
NEURODEVELOPMENTAL DISORDER WITH VISUAL DEFECTS AND BRAIN ANOMALIES  
NEURODEVELOPMENTAL, JAW, EYE, AND DIGITAL SYNDROME  
Neuromuscular Oculoauditory Syndrome  
ocular albinism +   
ocular hypertension +   
ocular hypotension +   
ocular motility disease +   
Ocular Neovascularization +   
ocular sarcoidosis 
ophthalmia nodosa 
ophthalmomyiasis 
optic nerve disease +   
orbital disease +   
Pancreas Agenesis, Dorsal 
philophthalmiasis 
Posterior Lumbosacral Vertebral Fusion with Blepharoptosis 
pupil disease +   
Radiation-Induced Abnormalities 
refractive error +   
Renal and Mullerian Duct Hypoplasia +   
Respiratory System Abnormalities +   
retinal disease +   
Rhiny 
Saito Kuba Tsuruta Syndrome 
Schlegelberger Grote Syndrome 
scleral disease +   
scotoma +   
situs inversus +   
Skin Abnormalities +   
Sprengel Deformity  
Stomatognathic System Abnormalities +   
thyroid malformation +   
toxocariasis +   
Urogenital Abnormalities +   
uveal disease +   
Vision Disorders +   
visual pathway disease +   
vitreous detachment +   
vitreous disease +   
ZAKI SYNDROME  
 aniridia +   
 Anophthalmia +   
 coloboma +   
 cryptophthalmia +   
 Ectopia Lentis +   
 hydrophthalmos +   
 microphthalmia +   

Synonyms
Exact Synonyms: ABNORMALITY OF THE EYE ;   OCULAR ANOMALIES ;   eye abnormality
Narrow Synonyms: ABNORMAL ANTERIOR EYE SEGMENT MORPHOLOGY
Primary IDs: MESH:D005124
Xrefs: HP:0004328 ;   MP:0005193
Definition Sources: MESH:D005124

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